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Issue 19, 2019
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Transition-metal-free regioselective construction of 1,5-diaryl-1,2,3-triazoles through dehydrative cycloaddition of alcohols with aryl azides mediated by SO2F2

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Abstract

A novel, simple and practical method for mild, efficient, cost-effective and regioselective synthesis of highly valuable 1,5-diaryl-1,2,3-triazoles was achieved through dehydrative annulation of readily available alcohols with aryl azides. The reaction proceeded at room temperature, without any metal catalysts, exhibiting excellent compatibility to a large variety of functional groups (>50 examples), resulting in up to quantitative yields.

Graphical abstract: Transition-metal-free regioselective construction of 1,5-diaryl-1,2,3-triazoles through dehydrative cycloaddition of alcohols with aryl azides mediated by SO2F2

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Article information


Submitted
06 Dec 2018
Accepted
06 Feb 2019
First published
07 Feb 2019

Chem. Commun., 2019,55, 2845-2848
Article type
Communication

Transition-metal-free regioselective construction of 1,5-diaryl-1,2,3-triazoles through dehydrative cycloaddition of alcohols with aryl azides mediated by SO2F2

X. Zhang, K. P. Rakesh and H. Qin, Chem. Commun., 2019, 55, 2845
DOI: 10.1039/C8CC09693G

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